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Top Online Casino is often accompanied by other immune disorders such as rheumatoid arthritis, lupus. Sjögren's syndrome first affects both the moisture-producing glands and mucous membranes, which eventually leads to a decrease in the amount of tears and saliva.

Although the disease can flare up at any age, most people are diagnosed over the age of 40. The disease is more common in women.

This syndrome also has one or more of the following symptoms:

joint pain, swelling, stiffness; swelling of the salivary glands; skin rash or dry skin; persistent dry cough; severe fatigue.

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Dressler's autoimmune syndrome is a secondary inflammation of the pericardium (pericarditis) or pleura (pleurisy) that occurs several weeks after a myocardial infarction or cardiac surgery.

Symptoms of Dressler's autoimmune syndrome: chest pain (stabbing in nature, aggravated by a deep breath, sometimes gives to the left shoulder); fever; dyspnea; pericardial effusion; atrial murmur; typical ECG changes; growth of inflammatory markers (CRP, leukocytosis, etc.).

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Werlhof's disease is idiopathic thrombocytopenic purpura or autoimmune thrombocytopenia.

Bleeding in this disease is caused by a decrease in the number of platelets (the reasons for the decrease in their number are still little known). About 90% of patients (mostly women) are younger than 25 years.

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The acute form is manifested by the following symptoms:

Autoimmune decussation syndrome is an unpleasant liver disease, the basis of USA Casino is chronic inflammation of the liver. The disease affects the liver tissue, causes deteriorationthe function of the liver. Autoantibodies attack liver cells, damage them, and cause chronic inflammation.

The course of the disease varies. Sometimes the overlap syndrome has the character of acute inflammation of the liver with expressive symptoms, including the following manifestations:

Autoimmune chiasm syndrome can lead to impaired liver function or chronic inflammation. lymphoproliferative syndrome. Autoimmune lymphoproliferative syndrome is a type of lymphoproliferative disorder resulting from impaired Fas-induced apoptosis of mature lymphocytes.

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Autoimmune lymphoproliferative syndrome is accompanied by the following clinical manifestations: thrombocytopenia; hemolytic anemia; lymphatic infiltration of T-lymphocytes (splenomegaly, chronic non-malignant lymphadenopathy). In this disease, there is an increased risk of developing lymphomas, severe attacks of immune cytopenia. The disease is rare.

Establishing the diagnosis of APS is based on the analysis of the anamnesis, clinical symptoms, objective finding and laboratory tests.

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Various types of drugs are used to treat certain diseases. The basis of therapy is the suppression of the human immune system through the use of immunosuppressants. The problem is that suppressing the immune system is dangerous due to the development of infections and cancer.
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Thus, immunodeficiency drugs are used under strict medical supervision! The exception is type 1 diabetes and other autoimmune diseases that affect the hormonal glands. In these cases, the patient is given the missing hormones (for casino online, insulin).
Of the drugs, corticosteroids are most often used, both in the form of tablets and in the form of skin ointments. However, immunosuppressants are more readily available; the use of a particular drug depends on the disease and its severity.

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